Senior Manager/Associate Director/Director/Senior Director
Job Responsibilities
1.Take lead or contribute to developing clinical development plan for the assigned project；
2.Accountable for clinical study protocol development and medical monitoring related activities；
3.Support preparation of study related documents (e.g. IB, study protocol, ICF, CRF, SMC charter, medical monitoring plan, SAP, CSR)；
4.Support clinical safety reviews and data analyses；
5. Interact and collaborate with external service providers and expert consultants.
Qualifications:
1.Medical degree (M.D.) with good medical knowledge and clinical experience in neurology or chronic pain, Master or Ph.D would be a plus；
2. At least 3 years of industry experience in clinical research；
3.Good command of English, both in written and spoken.
E-mail：hr@simrbio.com
